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PE Anti-Human CD86 Antibody[BU63]

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  • PE Anti-Human CD86 Antibody[BU63]-1
  • PE Anti-Human CD86 Antibody[BU63]-2
PE Anti-Human CD86 Antibody[BU63]-1

Staining of normal human peripheral blood cells with Anti-Human CD14 APC and Anti-Human CD86 PE (left) or Mouse IgG1, κ Isotype Control PE (right). Cells in the monocyte gate were used for analysis.

货号：GFH1012D

价格： ￥2736.00 ￥1080.00 ￥4104.00

规格：
100 Tests 20 Tests 100 Tests × 2
产品详情
Background

CD86 is an 80 kD immunoglobulin superfamily member also known as B7-2, B70, and Ly-58. CD86 is expressed on activated B and T cells, monocytes/macrophages, dendritic cells, and astrocytes. CD86, along with CD80, is the ligand of CD28 and CD152 (CTLA-4). CD86 is expressed earlier in the immune response than CD80. CD86 has also been shown to be involved in immunoglobulin class-switching and triggering of NK cell-mediated cytotoxicity. CD86 binds to CD28 to transduce costimulatory signals for T cell activation, proliferation, and cytokine production. CD86 can bind to CD152 as well, also known as CTLA-4, to deliver an inhibitory signal to T cells.

Alternate Names

Activation B7-2 antigen;Cd86;ETC-1;Early T-cell costimulatory molecule 1;T-lymphocyte activation antigen CD86

Clone No.

BU63

Host

Mouse

Reactivity

Human

Isotype

Mouse IgG1, κ

Conjugate

PE

Concentration

5 μL/Test

Applications

FCM

Clonality

Monoclonal

Storage Buffer

Phosphate buffered solution, pH 7.2, containing 0.09% sodium azide and 1% BSA.

Storage

This product can be stored at 2-8°C for 12 months. Please protected from prolonged exposure to light and do not freeze.

Expiration Date

12个月

Shipping

冰袋

产品结果图

Staining of normal human peripheral blood cells with Anti-Human CD14 APC and Anti-Human CD86 PE (left) or Mouse IgG1, κ Isotype Control PE (right). Cells in the monocyte gate were used for analysis.

PE Anti-Human CD86 Antibody[BU63]-产品结果图-1

Staining of normal human peripheral blood cells with Anti-Human CD14 APC and Anti-Human CD86 PE (left) or Mouse IgG1, κ Isotype Control PE (right). Cells in the monocyte gate were used for analysis.

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